ZMP
ENSDARG00000058782
Ensembl ID:
Alleles
There are 13 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22993 | Nonsense | Available for shipment | Available now |
sa17887 | Nonsense | Available for shipment | Available now |
sa22994 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22993
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081721 | Nonsense | 142 | 1871 | 4 | 40 |
Genomic Location (Zv9):
Chromosome 17 (position 6618210)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 6697146 |
GRCz11 | 17 | 6854376 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGTTTTGTCTCCTGAAGGATTCCGATCTTCATAAAGTGACCGATGCTT[T/G]AAAGCAGCTCATTACATCAGTTTGCCAACCAGAAGCTTCATCCCTTAAAG
Long Flanking Sequence:
TGTTTATGGAGTCTTCTCTACTAGTATAGCTGTTTAACCATGTGGATGGATGATAACAGCCTTCTGAGCCAACCAGTAAACGCAGATGGCCCCTACTGGCCCATATCTATAAGCTAATAACTACTGATAATACCCATTCAATCGAATGATAACATTCGAAGTAGGTGAACCAATGCTGAGCAGTCATTAGCAAAAATATTGTTCACTGTTAACGAATGCAGGATAATGCATTATAGGAATAGTTCATCCAAAAACTAAAATATTCGCATCATTTACTCACCCTCAAGTGCTTCCAATCCTTTATGAGTTAATTTATTCTGTCAAACACAAAAGAAGATATTTTGAAATATGTTAGAAAGCAAATACTCTGGAAGTCAGTGCTTTCATGTGAATGTTGGTCATTTTAAGTAACAGTGGAATTAGTCCTGTATCCAGCATTGCTCCACTGATGCTGTTTTGTCTCCTGAAGGATTCCGATCTTCATAAAGTGACCGATGCTT[T/G]AAAGCAGCTCATTACATCAGTTTGCCAACCAGAAGCTTCATCCCTTAAAGATACCTCTGATGTGTGGAGAAACATTTATAACACAGCAAACATGCTTCAGGTGAGTATCAGTAGAGAAATAGATGCTTTAAAATTATATTCTCAAGATCAACATAAAAGCACACTCAGTTTTTAAATACACGGTCCTATTGTGTTTTGTTTTTGGTTTAACGGTTCATTTAAAGCAGAGATGCCCAAAGGTGGCCCATGTTAACCTTTCATTTGGCATGCCATCCAATTGTCTTGTCAATTTTAATGTAATTTTTTTAATAAATGCTGAGCTACAAAAAATAGCCACTCTGTCACTTGACTGAAAGATGCAGAAGAAATGCAAAAGAAATTCGTGAGCAAATTAAGCCACAGATCAACTAGTAGTGTATTCCACTTTGGGATTATTTCTGTTTTTAGTGCAGTAATTTCATTATAAAATGATACCGCATTATTACTTAATATGATTTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17887
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081721 | Nonsense | 168 | 1871 | 4 | 40 |
Genomic Location (Zv9):
Chromosome 17 (position 6618289)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 6697225 |
GRCz11 | 17 | 6854455 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCAGAAGCTTCATCCCTKAAAGATACCTCTGATGTGTGGAGAAACATTTA[T/G]AACACAGCAAACATGYTYCAGGTGAGTATCAGTAGAGAAATAGATGCTTT
Long Flanking Sequence:
ACGCAGATGGCCCCTACTGGCCCATATCTATAAGCTAATAACTACTGATAATACCCATTCAATCGAATGATAACATTCGAAGTAGGTGAACCAATGCTGAGCAGTCATTAGCAAAAATATTGTTCACTGTTAACGAATGCAGGATAATGCATTATAGGAATAGTTCATCCAAAAACTAAAATATTCGCATCATTTACTCACCCTCAAGTGCTTCCAATCCTTTATGAGTTAATTTATTCTGTCAAACACAAAAGAAGATATTTTGAAATATGTTAGAAAGCAAATACTCTGGAAGTCAGTGCTTTCATGTGAATGTTGGTCATTTTAAGTAACAGTGGAATTAGTCCTGTATCCAGCATTGCTCCACTGATGCTGTTTTGTCTCCTGAAGGATTCCGATCTTCATAAAGTGACCGATGCTTTAAAGCAGCTCATTACATCAGTTTGCCAACCAGAAGCTTCATCCCTTAAAGATACCTCTGATGTGTGGAGAAACATTTA[T/G]AACACAGCAAACATGCTTCAGGTGAGTATCAGTAGAGAAATAGATGCTTTAAAATTATATTCTCAAGATCAACATAAAAGCACACTCAGTTTTTAAATACACGGTCCTATTGTGTTTTGTTTTTGGTTTAACGGTTCATTTAAAGCAGAGATGCCCAAAGGTGGCCCATGTTAACCTTTCATTTGGCATGCCATCCAATTGTCTTGTCAATTTTAATGTAATTTTTTTAATAAATGCTGAGCTACAAAAAATAGCCACTCTGTCACTTGACTGAAAGATGCAGAAGAAATGCAAAAGAAATTCGTGAGCAAATTAAGCCACAGATCAACTAGTAGTGTATTCCACTTTGGGATTATTTCTGTTTTTAGTGCAGTAATTTCATTATAAAATGATACCGCATTATTACTTAATATGATTTAAAGCAACGTTTTCTAGTTATTTTTAAATATTTGCAAATAAATTAGGAAATTACGAATGGTAAATTTAATGTAATACAGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22994
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081721 | Essential Splice Site | 715 | 1871 | 15 | 40 |
Genomic Location (Zv9):
Chromosome 17 (position 6641707)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 6720643 |
GRCz11 | 17 | 6877873 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACAGTTGGAAAATACATTCTTGTTGATTTTGGCTTCTTTCTTTTTTTCT[A/G]GGTTTATCCCAAACAGTCTTCCTCTTGCTGTTCAGGAACTTGATGAAAAT
Long Flanking Sequence:
ACTAGCTTATAGAGATCCTTAAAACTAACATACTGATACTAATGTCTACAAAAAAACTTTATCTTAATTTCATGGAACCTTTAAAACCAACCAACTACAGTAGGTGTTTTGCAGCCTCAATGCTGTAATCAGTAGTTGTTTTCAAGTCCAGGATGAGTATTTAACAAGATTTAGGAGCCGTTCACTTTTACACTTTTCACGCTTTTACTGTTAACATACCTAATTCTTTAAAAACTTTGTGTAAATGTGCTCTAGGAAATATTTTTTAATTATTCGTACTAATTTATTTTGTGCCTTTTGCTATTTTTCCTTCATATTCTGTGAGCAGCTACTATACCAAAATGAGGTAGCATAATCAAAAGCTGTTCATTTGAGGTACTTGAGCTCAATCACTCAAACATCGAATACAATTTTTTTCAAAGCACTTCACAGGACCTTTAAGTTTTCTTGAACAGTTGGAAAATACATTCTTGTTGATTTTGGCTTCTTTCTTTTTTTCT[A/G]GGTTTATCCCAAACAGTCTTCCTCTTGCTGTTCAGGAACTTGATGAAAATCATATCTGCAAATTCAGCTTTCGATCGAAAGAAGCAGTTTTACAGGTAATTACACAATGATTGACAACACAGGTCTGTGTCTGGGAAGAAAATCTGATGATGTTTCAAACAAAACAAAGCAAAATTTTGTTTCTAAACTTGCATGAGTTTCTTTTTTCTGCTAAAACCAAAAGAAAATATTCTGAAGAATGTTGGAAACCAAAAAAATGCATGGTCCTCACTGACTTTCATAGTAAGTGACTAAAAATACCATTTCAGTCAAAAGGGGACCAACAACTGTGTGCTTTCCAACATTCTTCGAAATAACTTCTTTTGTGTTTTTTTATTTTTATTTTTAATTGTAGCATCCCTACAAGTGATTAATATTTCTCCATCTTTTTAAAAAGGCCACAAAATGCCATATATTGTGAGGAATTTCATGAAGAACAAAGCAGTTATGATTATTGGAAT
Associated Phenotype:
Not determined